Variant report

Variant	nsv1006471
Chromosome Location	chr3:21385627-21596955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:978)
CpG islands
(count:671)
Chromatin interactive
region (count:74)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:21573683-21573857	K562	blood:	n/a	n/a
2	ARID3A	chr3:21573306-21573327	K562	blood:	n/a	n/a
3	ARID3A	chr3:21592635-21592859	K562	blood:	n/a	n/a
4	ARID3A	chr3:21567931-21568332	K562	blood:	n/a	n/a
5	ARID3A	chr3:21528483-21528486	K562	blood:	n/a	n/a
6	ARID3A	chr3:21581435-21581446	K562	blood:	n/a	n/a
7	ATF1	chr3:21568030-21568242	K562	blood:	n/a	n/a
8	ATF1	chr3:21440459-21440632	K562	blood:	n/a	n/a
9	ATF1	chr3:21573428-21573805	K562	blood:	n/a	n/a
10	ATF1	chr3:21592604-21592903	K562	blood:	n/a	n/a
11	ATF2	chr3:21487560-21487918	GM12878	blood:	n/a	n/a
12	ATF3	chr3:21447160-21447359	K562	blood:	n/a	n/a
13	BACH1	chr3:21558769-21558830	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr3:21487397-21487659	GM12878	blood:	n/a	n/a
15	BATF	chr3:21526355-21526594	GM12878	blood:	n/a	chr3:21526456-21526467
16	BCL11A	chr3:21585006-21585200	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr3:21487425-21487837	GM12878	blood:	n/a	chr3:21487787-21487796
18	BHLHE40	chr3:21589714-21589739	K562	blood:	n/a	n/a
19	BHLHE40	chr3:21584305-21584749	K562	blood:	n/a	n/a
20	BHLHE40	chr3:21573457-21573641	K562	blood:	n/a	n/a
21	BHLHE40	chr3:21487490-21487873	GM12878	blood:	n/a	n/a
22	BHLHE40	chr3:21592657-21592899	K562	blood:	n/a	n/a
23	BRCA1	chr3:21526090-21526158	GM12878	blood:	n/a	n/a
24	BRCA1	chr3:21483405-21483415	GM12878	blood:	n/a	n/a
25	BRCA1	chr3:21558865-21558897	HepG2	liver:	n/a	n/a
26	CBX3	chr3:21583994-21584381	K562	blood:	n/a	n/a
27	CBX3	chr3:21573374-21573782	K562	blood:	n/a	n/a
28	CBX3	chr3:21447117-21447403	K562	blood:	n/a	n/a
29	CCNT2	chr3:21567997-21568235	K562	blood:	n/a	n/a
30	CCNT2	chr3:21572196-21572328	K562	blood:	n/a	n/a
31	CCNT2	chr3:21468599-21468799	K562	blood:	n/a	n/a
32	CEBPB	chr3:21404484-21404623	K562	blood:	n/a	n/a
33	CEBPB	chr3:21573406-21573812	K562	blood:	n/a	n/a
34	CEBPB	chr3:21567992-21568334	Hela-S3	cervix:	n/a	chr3:21568162-21568173
35	CEBPB	chr3:21551220-21551548	IMR90	lung:	n/a	chr3:21551381-21551392 chr3:21551403-21551412 chr3:21551401-21551414 chr3:21551382-21551391 chr3:21551402-21551413
36	CEBPB	chr3:21492820-21493030	HepG2	liver:	n/a	chr3:21492857-21492874
37	CEBPB	chr3:21573522-21573817	K562	blood:	n/a	n/a
38	CEBPB	chr3:21567806-21568423	K562	blood:	n/a	chr3:21568162-21568173
39	CEBPB	chr3:21546923-21547244	K562	blood:	n/a	n/a
40	CEBPB	chr3:21452758-21453387	HepG2	liver:	n/a	chr3:21453014-21453025 chr3:21453014-21453025 chr3:21453014-21453027 chr3:21453254-21453265
41	CEBPB	chr3:21551240-21551571	Hela-S3	cervix:	n/a	chr3:21551381-21551392 chr3:21551403-21551412 chr3:21551401-21551414 chr3:21551382-21551391 chr3:21551402-21551413
42	CEBPB	chr3:21585278-21585530	K562	blood:	n/a	n/a
43	CEBPB	chr3:21551287-21551545	K562	blood:	n/a	chr3:21551381-21551392 chr3:21551403-21551412 chr3:21551401-21551414 chr3:21551382-21551391 chr3:21551402-21551413
44	CEBPB	chr3:21551215-21551562	HepG2	liver:	n/a	chr3:21551381-21551392 chr3:21551403-21551412 chr3:21551401-21551414 chr3:21551382-21551391 chr3:21551402-21551413
45	CEBPB	chr3:21574708-21574853	K562	blood:	n/a	n/a
46	CEBPB	chr3:21567962-21568282	K562	blood:	n/a	chr3:21568162-21568173
47	CEBPB	chr3:21495673-21495929	HepG2	liver:	n/a	chr3:21495766-21495777
48	CEBPB	chr3:21472711-21472916	A549	lung:	n/a	chr3:21472831-21472848
49	CEBPB	chr3:21403738-21403864	A549	lung:	n/a	n/a
50	CEBPB	chr3:21453141-21453424	A549	lung:	n/a	chr3:21453254-21453265

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:21558209-21558259	SAEC	small airway:	n/a
2	chr3:21447667-21447717	HUVEC	blood vessel:	n/a
3	chr3:21445979-21446029	PFSK-1	brain:	n/a
4	chr3:21446874-21446924	SK-N-SH	brain:	n/a
5	chr3:21558209-21558259	HCT-116	colon:	n/a
6	chr3:21558209-21558259	HCPEpiC	choroid plexus:	n/a
7	chr3:21584249-21584299	NB4	blood:	n/a
8	chr3:21448049-21448099	NB4	blood:	n/a
9	chr3:21558209-21558259	CMK	blood:	n/a
10	chr3:21426059-21426109	GM19239	blood:	n/a
11	chr3:21447391-21447441	SKMC	muscle:	n/a
12	chr3:21447501-21447551	Hepatocyte	liver:	n/a
13	chr3:21448049-21448099	SK-N-SH_RA	brain:	n/a
14	chr3:21558209-21558259	GM12891	blood:	n/a
15	chr3:21448012-21448062	NHDF-neo	bronchial:	n/a
16	chr3:21447501-21447551	CMK	blood:	n/a
17	chr3:21447667-21447717	SK-N-SH	brain:	n/a
18	chr3:21447501-21447551	MCF10A-Er-Src	breast:	n/a
19	chr3:21426059-21426109	CMK	blood:	n/a
20	chr3:21426059-21426109	NHDF-neo	bronchial:	n/a
21	chr3:21447391-21447441	NT2-D1	testis:	n/a
22	chr3:21447667-21447717	IMR90	lung:	fetal
23	chr3:21447667-21447717	PrEC	prostate:	n/a
24	chr3:21448049-21448099	GM06990	blood:	n/a
25	chr3:21446874-21446924	GM12878	blood:	n/a
26	chr3:21446874-21446924	NT2-D1	testis:	n/a
27	chr3:21446874-21446924	PrEC	prostate:	n/a
28	chr3:21447667-21447717	HepG2	liver:	n/a
29	chr3:21448049-21448099	HAEpiC	amniotic membrane:	n/a
30	chr3:21445979-21446029	T-47D	breast:	n/a
31	chr3:21445979-21446029	HL-60	blood:	n/a
32	chr3:21447667-21447717	HCPEpiC	choroid plexus:	n/a
33	chr3:21584249-21584299	AoSMC	blood vessel:	n/a
34	chr3:21447508-21447558	GM12891	blood:	n/a
35	chr3:21558209-21558259	AG09319	gingival:	n/a
36	chr3:21584249-21584299	HMEC	breast:	n/a
37	chr3:21558209-21558259	A549	lung:	n/a
38	chr3:21447501-21447551	HEEpiC	esophagus:	n/a
39	chr3:21426059-21426109	AG09319	gingival:	n/a
40	chr3:21447667-21447717	Caco-2	colon:	n/a
41	chr3:21448049-21448099	Jurkat	blood:	n/a
42	chr3:21446874-21446924	HEK293	kidney:	embryo
43	chr3:21584249-21584299	MCF10A-Er-Src	breast:	n/a
44	chr3:21447501-21447551	SAEC	small airway:	n/a
45	chr3:21447667-21447717	HCT-116	colon:	n/a
46	chr3:21446874-21446924	HIPEpiC	eye:	n/a
47	chr3:21447391-21447441	NHDF-neo	bronchial:	n/a
48	chr3:21447667-21447717	SKMC	muscle:	n/a
49	chr3:21447667-21447717	HRE	kidney:	n/a
50	chr3:21447501-21447551	IMR90	lung:	fetal

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:21439366..21441034-chr3:21442770..21445274,2	K562	blood:
2	chr3:21558303..21559979-chr3:21581048..21584024,2	K562	blood:
3	chr3:21431277..21433806-chr3:21435047..21437239,3	K562	blood:
4	chr3:19926567..19927530-chr3:21592329..21593167,2	MCF-7	breast:
5	chr3:21466338..21470140-chr3:21472004..21475648,4	K562	blood:
6	chr3:21573606..21577614-chr3:21581986..21586764,5	K562	blood:
7	chr3:21534337..21537084-chr3:21554573..21557096,2	K562	blood:
8	chr3:21547308..21549346-chr3:21549742..21551685,2	K562	blood:
9	chr3:21572284..21575106-chr3:21582629..21584216,2	K562	blood:
10	chr3:21446128..21447988-chr3:21449593..21451314,2	K562	blood:
11	chr3:21491005..21492571-chr3:21495896..21498520,2	K562	blood:
12	chr3:21533469..21535837-chr3:21555368..21557096,2	K562	blood:
13	chr3:21388598..21390467-chr3:21391576..21393925,2	K562	blood:
14	chr3:20381671..20382483-chr3:21592493..21593315,3	MCF-7	breast:
15	chr3:21508162..21510011-chr3:21513396..21515534,2	K562	blood:
16	chr3:21386176..21388301-chr3:21404995..21407589,2	K562	blood:
17	chr3:21448531..21452327-chr3:21453436..21457568,4	K562	blood:
18	chr3:21525648..21526262-chr3:21592336..21593160,2	MCF-7	breast:
19	chr3:21508162..21510011-chr3:21513396..21515534,2	K562	blood:
20	chr3:21438293..21442012-chr3:21443506..21445713,3	K562	blood:
21	chr3:21565324..21568095-chr3:21579893..21581736,2	K562	blood:
22	chr3:21511527..21513204-chr3:21517640..21519938,2	K562	blood:
23	chr3:21565741..21568055-chr3:21571417..21573750,2	K562	blood:
24	chr3:21431277..21433806-chr3:21435047..21437239,3	K562	blood:
25	chr3:21577254..21579232-chr3:21580872..21582728,2	K562	blood:
26	chr3:21388282..21390460-chr3:21398661..21400819,2	K562	blood:
27	chr3:21386176..21388301-chr3:21404995..21407589,2	K562	blood:
28	chr3:21572284..21575106-chr3:21582629..21584216,2	K562	blood:
29	chr3:21551694..21553640-chr3:21557602..21559224,2	K562	blood:
30	chr3:21541046..21543209-chr3:21550142..21552460,2	K562	blood:
31	chr3:21491005..21492571-chr3:21495896..21498520,2	K562	blood:
32	chr3:21438293..21442012-chr3:21443506..21445713,3	K562	blood:
33	chr3:21388598..21390467-chr3:21391576..21393925,2	K562	blood:
34	chr3:21058134..21059174-chr3:21592293..21593050,3	MCF-7	breast:
35	chr3:21558303..21559979-chr3:21581048..21584024,2	K562	blood:
36	chr3:21381102..21383225-chr3:21383828..21386655,2	MCF-7	breast:
37	chr3:21058395..21059158-chr3:21525879..21526450,3	MCF-7	breast:
38	chr3:20378280..20380658-chr3:21571258..21574044,2	K562	blood:
39	chr3:21565324..21568095-chr3:21579893..21581736,2	K562	blood:
40	chr3:21439015..21441958-chr3:21447248..21448760,2	K562	blood:
41	chr3:21554662..21556901-chr3:21563061..21566004,2	K562	blood:
42	chr3:21434215..21436621-chr3:21438277..21440578,2	MCF-7	breast:
43	chr3:21534337..21537084-chr3:21554573..21557096,2	K562	blood:
44	chr3:21439015..21441958-chr3:21447248..21448760,2	K562	blood:
45	chr3:21593555..21596291-chr3:21602038..21604298,2	K562	blood:
46	chr3:21554662..21556901-chr3:21563061..21566004,2	K562	blood:
47	chr3:21547308..21549346-chr3:21549742..21551685,2	K562	blood:
48	chr3:21388282..21390460-chr3:21398661..21400819,2	K562	blood:
49	chr3:21533469..21535837-chr3:21555368..21557096,2	K562	blood:
50	chr3:21426737..21428480-chr3:21430250..21431910,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-4	chr3:21584308-21584487	ENSG00000225542.1
2	lnc-ZNF385D-1	chr3:21453714-21455436	ENSG00000272511.1

No data

Variant related genes	Relation type
VENTXP7	TF binding region
ZNF385D-AS1	TF binding region
ENSG00000252306	TF binding region
ZNF385D	TF binding region
ENSG00000272511	TF binding region
VENTXP7	CpG island
ZNF385D-AS1	CpG island
ENSG00000252306	CpG island
ZNF385D	CpG island
ENSG00000272511	CpG island
ENSG00000236380	chromatin interactions
ENSG00000151789	chromatin interactions
ENSG00000225542	chromatin interactions
ENSG00000272511	chromatin interactions

Extended variants
information (count: 7467 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:7467 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538013825	chr3:21386849-21386850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs188818253	chr3:21386930-21386931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573134907	chr3:21386962-21386963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs149991175	chr3:21386987-21386988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191710129	chr3:21387032-21387033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs545016921	chr3:21387044-21387045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185382082	chr3:21387088-21387089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369082442	chr3:21387112-21387113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113159611	chr3:21387127-21387128	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371209381	chr3:21387128-21387129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371174196	chr3:21387129-21387130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs61191084	chr3:21387148-21387149	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs68134541	chr3:21387149-21387150	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7650614	chr3:21387151-21387152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542700981	chr3:21387152-21387153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs367908358	chr3:21387155-21387156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550535030	chr3:21387156-21387157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555570469	chr3:21387170-21387171	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561591752	chr3:21387184-21387185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs529086705	chr3:21387203-21387204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544034357	chr3:21387236-21387237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs562826125	chr3:21387266-21387267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs111472795	chr3:21387399-21387400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189724096	chr3:21397436-21397437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549166432	chr3:21397481-21397482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181183148	chr3:21397498-21397499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530944459	chr3:21397553-21397554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552577636	chr3:21397577-21397578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564598564	chr3:21397651-21397652	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369922787	chr3:21397653-21397654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547315428	chr3:21397655-21397656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552925389	chr3:21397738-21397739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565863586	chr3:21397742-21397743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13095327	chr3:21397755-21397756	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs548085441	chr3:21397791-21397792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186159423	chr3:21397862-21397863	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs538083949	chr3:21397873-21397874	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs551691546	chr3:21397894-21397895	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs376997409	chr3:21397900-21397901	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs576573480	chr3:21397916-21397917	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs534716292	chr3:21397944-21397945	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs145512020	chr3:21397972-21397973	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs116451180	chr3:21397985-21397986	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs542024420	chr3:21397991-21397992	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs563995289	chr3:21398011-21398012	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs33998065	chr3:21398020-21398021	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs575984961	chr3:21398104-21398105	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs188913663	chr3:21398105-21398106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181932186	chr3:21398139-21398140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528625122	chr3:21398155-21398156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21386800-21387400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr3:21397400-21397600	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr3:21397400-21397800	Enhancers	NHDF-Ad	bronchial
4	chr3:21397600-21398400	Enhancers	Muscle Satellite Cultured Cells	--
5	chr3:21397600-21398400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr3:21397600-21398600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr3:21397800-21398000	Flanking Active TSS	NHDF-Ad	bronchial
8	chr3:21398000-21398200	Enhancers	NHDF-Ad	bronchial
9	chr3:21398200-21398400	Flanking Active TSS	NHDF-Ad	bronchial
10	chr3:21398400-21399000	Enhancers	NHDF-Ad	bronchial
11	chr3:21398600-21399400	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr3:21398800-21399200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr3:21398800-21399200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr3:21413400-21413800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:21413800-21414200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:21413800-21414400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr3:21413800-21414600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr3:21414000-21414600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr3:21414200-21414400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:21414400-21414600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:21414600-21414800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:21414600-21418200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:21414800-21418000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:21418000-21419200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:21418200-21418800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr3:21418600-21420000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr3:21418800-21420200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr3:21420200-21420400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr3:21424000-21424200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr3:21424200-21432800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr3:21425400-21426400	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr3:21426200-21426800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr3:21426800-21427800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
34	chr3:21428800-21429200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr3:21429200-21431800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:21430400-21431800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr3:21431000-21431600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr3:21431200-21432000	Enhancers	Rectal Smooth Muscle	rectum
39	chr3:21431200-21432200	Enhancers	Muscle Satellite Cultured Cells	--
40	chr3:21431200-21432200	Enhancers	NHDF-Ad	bronchial
41	chr3:21431200-21432800	Enhancers	NH-A	brain
42	chr3:21431200-21435400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr3:21431600-21432000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:21431800-21432000	Enhancers	Aorta	Aorta
45	chr3:21431800-21432200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr3:21431800-21432600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr3:21431800-21433600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr3:21432000-21435200	Weak transcription	Aorta	Aorta
49	chr3:21432200-21433800	Weak transcription	NHDF-Ad	bronchial
50	chr3:21432200-21435400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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